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3,648 results on '"Ludolph, Albert C"'

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1. Clinical characterization of common pathogenic variants of SOD1-ALS in Germany

7. Economic evaluation of Motor Neuron Diseases: a nationwide cross-sectional analysis in Germany

9. Structural parameters are superior to eigenvector centrality in detecting progressive supranuclear palsy with machine learning & multimodal MRI

10. Safety and efficacy of arimoclomol in patients with early amyotrophic lateral sclerosis (ORARIALS-01): a randomised, double-blind, placebo-controlled, multicentre, phase 3 trial

13. Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study

16. Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes

17. Cystatin C based estimation of chronic kidney disease and amyotrophic lateral sclerosis in the ALS registry Swabia: associated risk and prognostic value

23. Integrative genetic analysis illuminates ALS heritability and identifies risk genes

24. Tau-targeting antisense oligonucleotide MAPTRx in mild Alzheimer’s disease: a phase 1b, randomized, placebo-controlled trial

25. Loss of hypothalamic MCH decreases food intake in amyotrophic lateral sclerosis

28. Patient-reported outcome parameters and disability worsening in progressive multiple sclerosis

29. Author Correction: Tau-targeting antisense oligonucleotide MAPTRx in mild Alzheimer’s disease: a phase 1b, randomized, placebo-controlled trial

30. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

33. Effect of the addition of a mental health specialist for evaluation of undiagnosed patients in centres for rare diseases (ZSE-DUO): a prospective, controlled trial with a two-phase cohort design

38. Blood–CSF barrier integrity in amyotrophic lateral sclerosis

46. Use and subjective experience of the impact of motor-assisted movement exercisers in people with amyotrophic lateral sclerosis: a multicenter observational study

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